PE20121031A1 - Nuevos conjugados, su preparacion y su aplicacion terapeutica - Google Patents

Nuevos conjugados, su preparacion y su aplicacion terapeutica

Info

Publication number
PE20121031A1
PE20121031A1 PE2011002178A PE2011002178A PE20121031A1 PE 20121031 A1 PE20121031 A1 PE 20121031A1 PE 2011002178 A PE2011002178 A PE 2011002178A PE 2011002178 A PE2011002178 A PE 2011002178A PE 20121031 A1 PE20121031 A1 PE 20121031A1
Authority
PE
Peru
Prior art keywords
methyl
etoxy
phenyl
alkyl
mercapto
Prior art date
Application number
PE2011002178A
Other languages
English (en)
Inventor
Herve Bouchard
Marie-Priscille Brun
Alain Commerçon
Jidong Zhang
Original Assignee
Sanofi Sa
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41611078&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20121031(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sanofi Sa filed Critical Sanofi Sa
Publication of PE20121031A1 publication Critical patent/PE20121031A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D273/00Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
    • C07D273/08Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00 having two nitrogen atoms and more than one oxygen atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D245/00Heterocyclic compounds containing rings of more than seven members having two nitrogen atoms as the only ring hetero atoms
    • C07D245/04Heterocyclic compounds containing rings of more than seven members having two nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
    • C07D245/06Heterocyclic compounds containing rings of more than seven members having two nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems condensed with one six-membered ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicinal Preparation (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Peptides Or Proteins (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

REFERIDA A UN COMPUESTO DE FORMULA I, DONDE R1 ES HALOGENO; R2 ES OH, ACILO DERIVADO DE UN AMINOACIDO NATURAL O NO NATURAL, ALCANOILOXI C1-C4 o R1 Y R2 FORMAN UN EPOXIDO; R3 ES ALQUILO C1-C6; R4 Y R5 SON CADA UNO H o FORMAN JUNTOS UN CH=CH ENTRE C13 Y C14; R6 Y R7 SON CADA UNO H, ALQUILO C1-C6; R8 Y R9 SON CADA UNO H, ALQUILO C1-C6; R10 ES H, OH, ALCOXI C1-C4, HALOGENO, ENTRE OTROS; R11 ES H, ALQUILO C1-C4; L ES UN CONECTOR DE PREFERENCIA EN POSICION PARA ELEGIDO ENTRE (4-MERCAPTO-4-METILPENTANOIL)-PIPERAZIN-1-ILMETIL-FENIL, [(2-MERCAPTO-2-METIL-PROPILAMINO)-METIL]-FENIL, 4-[4-({2-[2-(2-{2-METIL-[2-MERCAPTO-2-METIL-PROPIL]-AMINO-ETOXI}-ETOXI)-ETOXI]-ETIL}-METILAMINO)-METIL]FENIL, ENTRE OTROS. REFERIDO ADEMAS A UN DERIVADO DE CRPTOFICINA. UN COMPUESTO PREFERIDO: (E)-(3S,10R,16S)-10-(3-CLORO-4-METOXIBENCIL)-3-ISOBUTIL-16-[(S)-1-((2R,3R)-3-{4-[4-({2-[2-(2-{4-METIL-4-METILDISULFANIL-PENTANOILAMINO-ETOXI}-ETOXI)-ETOXI]-ETIL}METILAMINO)-METIL]-FENIL}-OXIRANIL)-ETIL]-6,6-DIMETIL-1,4-DIOXA-8,11-DIAZA-CICLOHEXADEC-13-ENO-2,5,9,12-TETRAONA. DICHOS COMPUESTOS SON UTILES EN EL TRATAMIENTO DEL CANCER
PE2011002178A 2009-06-29 2010-05-20 Nuevos conjugados, su preparacion y su aplicacion terapeutica PE20121031A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0903170A FR2947269B1 (fr) 2009-06-29 2009-06-29 Nouveaux composes anticancereux
FR0905651A FR2947271B1 (fr) 2009-06-29 2009-11-25 Nouveaux composes anticancereux

Publications (1)

Publication Number Publication Date
PE20121031A1 true PE20121031A1 (es) 2012-08-17

Family

ID=41611078

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2011002178A PE20121031A1 (es) 2009-06-29 2010-05-20 Nuevos conjugados, su preparacion y su aplicacion terapeutica

Country Status (30)

Country Link
US (1) US8952147B2 (es)
EP (1) EP2448929A1 (es)
JP (1) JP5746692B2 (es)
KR (1) KR101770584B1 (es)
CN (1) CN102482238B (es)
AR (1) AR078131A1 (es)
BR (1) BRPI1015131A2 (es)
CA (1) CA2766762C (es)
CL (1) CL2011003229A1 (es)
CO (1) CO6430462A2 (es)
CR (1) CR20110670A (es)
DO (1) DOP2011000376A (es)
EA (1) EA024627B1 (es)
EC (1) ECSP11011553A (es)
FR (2) FR2947269B1 (es)
HN (1) HN2011003414A (es)
IL (1) IL217208A (es)
MA (1) MA33465B1 (es)
MX (1) MX2011013764A (es)
MY (1) MY156684A (es)
NI (1) NI201100219A (es)
NZ (1) NZ597136A (es)
PE (1) PE20121031A1 (es)
SG (2) SG10201607595WA (es)
SV (1) SV2011004086A (es)
TN (1) TN2011000636A1 (es)
TW (1) TW201110986A (es)
UY (1) UY32745A (es)
WO (1) WO2011001052A1 (es)
ZA (1) ZA201109537B (es)

Families Citing this family (52)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3539572A1 (en) 2005-08-24 2019-09-18 ImmunoGen, Inc. Process for preparing maytansinoid antibody conjugates
EP2437790B1 (en) 2009-06-03 2019-02-20 Immunogen, Inc. Conjugation methods
EP2845856A1 (en) 2009-06-29 2015-03-11 Incyte Corporation Pyrimidinones as PI3K inhibitors
US8759359B2 (en) 2009-12-18 2014-06-24 Incyte Corporation Substituted heteroaryl fused derivatives as PI3K inhibitors
EP2558463A1 (en) 2010-04-14 2013-02-20 Incyte Corporation Fused derivatives as i3 inhibitors
WO2011163195A1 (en) 2010-06-21 2011-12-29 Incyte Corporation Fused pyrrole derivatives as pi3k inhibitors
TW201249844A (en) 2010-12-20 2012-12-16 Incyte Corp N-(1-(substituted-phenyl)ethyl)-9H-purin-6-amines as PI3K inhibitors
WO2012125629A1 (en) 2011-03-14 2012-09-20 Incyte Corporation Substituted diamino-pyrimidine and diamino-pyridine derivatives as pi3k inhibitors
US9126948B2 (en) 2011-03-25 2015-09-08 Incyte Holdings Corporation Pyrimidine-4,6-diamine derivatives as PI3K inhibitors
TR201902180T4 (tr) 2011-03-29 2019-03-21 Immunogen Inc Tek adimli bi̇r i̇şlem i̇le maytansi̇noi̇d anti̇kor konjugatlarinin hazirlanmasi
UA121539C2 (uk) 2011-09-02 2020-06-25 Інсайт Холдинґс Корпорейшн Гетероцикліламіни як інгібітори рі3к
AR090548A1 (es) 2012-04-02 2014-11-19 Incyte Corp Azaheterociclobencilaminas biciclicas como inhibidores de pi3k
RU2661083C2 (ru) 2012-10-04 2018-07-11 Иммуноджен, Инк. Использование пвдф-мембраны для очистки конъюгатов клеточно-связывающий агент - цитотоксический агент
HRP20170743T1 (hr) 2012-11-20 2017-07-28 Sanofi Anti-ceacam5 protutijela i njihova uporaba
BR112016000585A2 (pt) 2013-07-11 2018-03-20 Novartis Ag modificações quimioenzimáticas sítio-específicas de proteína
US10077277B2 (en) 2014-06-11 2018-09-18 Incyte Corporation Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors
PT3189056T (pt) * 2014-09-03 2020-09-04 Immunogen Inc Derivados citotóxicos de benzodiazepina
GB201416960D0 (en) 2014-09-25 2014-11-12 Antikor Biopharma Ltd Biological materials and uses thereof
UA122332C2 (uk) 2015-02-27 2020-10-26 Інсайт Корпорейшн Солі інгібітора pi3k і способи їх отримання
EP3069734A1 (en) * 2015-03-17 2016-09-21 Exiris S.r.l. Cryptophycin-based antibody-drug conjugates with novel self-immolative linkers
WO2016183060A1 (en) 2015-05-11 2016-11-17 Incyte Corporation Process for the synthesis of a phosphoinositide 3-kinase inhibitor
WO2016183063A1 (en) 2015-05-11 2016-11-17 Incyte Corporation Crystalline forms of a pi3k inhibitor
CN107029242A (zh) 2015-11-03 2017-08-11 财团法人工业技术研究院 抗体药物复合物及其制造方法
TWI714661B (zh) 2015-11-05 2021-01-01 法商賽諾菲公司 新穎念珠藻素化合物及接合物、其製備與其治療用途
WO2017136769A1 (en) * 2016-02-04 2017-08-10 Eisai R&D Management Co., Ltd. Peptide drug conjugates
AU2016429272A1 (en) 2016-11-14 2019-05-02 Hangzhou Dac Biotech Co., Ltd. Conjugation linkers, cell binding molecule-drug conjugates containing the likers, methods of making and uses such conjugates with the linkers
WO2018178277A1 (en) 2017-03-29 2018-10-04 Avicenna Oncology Gmbh New targeted cytotoxic isocombretaquinoline derivatives and conjugates thereof
AU2018265333C1 (en) 2017-05-10 2025-04-24 Sanofi Peptidic linkers and cryptophycin conjugates, useful in therapy, and their preparation
WO2019030284A1 (en) 2017-08-09 2019-02-14 Helmholtz-Zentrum für Infektionsforschung GmbH NOVEL TARGETED CYTOTOXIC RATJADONE DERIVATIVES AND CONJUGATES THEREOF
AU2018389100B2 (en) * 2017-12-22 2025-02-27 Cornell University 18F-labeled peptide ligands useful in PET and Cerenkov luminescene imaging
MX2020012826A (es) 2018-06-01 2021-03-09 Incyte Corp Regimen de dosificacion para el tratamiento de trastornos relacionados con fosfatidilinositol 3-cinasas (pi3k).
US12018087B2 (en) 2018-08-02 2024-06-25 Dyne Therapeutics, Inc. Muscle-targeting complexes comprising an anti-transferrin receptor antibody linked to an oligonucleotide and methods of delivering oligonucleotide to a subject
JP7611825B2 (ja) 2018-08-02 2025-01-10 ダイン セラピューティクス,インコーポレーテッド ジストロフィン異常症を処置するための筋標的化複合体およびそれらの使用
US11168141B2 (en) 2018-08-02 2021-11-09 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating dystrophinopathies
US12097263B2 (en) 2018-08-02 2024-09-24 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating myotonic dystrophy
US20220193250A1 (en) 2018-08-02 2022-06-23 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating facioscapulohumeral muscular dystrophy
US12370264B1 (en) 2018-08-02 2025-07-29 Dyne Therapeutics, Inc. Complexes comprising an anti-transferrin receptor antibody linked to an oligonucleotide and method of delivering oligonucleotide to a subject
US11911484B2 (en) 2018-08-02 2024-02-27 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating myotonic dystrophy
FR3085952B1 (fr) 2018-09-17 2020-10-30 Centre Nat Rech Scient Conjugue anticorps-medicament comprenant des derives de quinoline
WO2021067460A1 (en) 2019-09-30 2021-04-08 The Regents Of The University Ofmichigan Biocatalytic synthesis of cryptophycin anticancer agents
US12624120B2 (en) 2020-01-31 2026-05-12 Dyne Therapeutics, Inc. Anti-transferrin receptor (TfR) antibody and uses thereof
US12564642B2 (en) 2020-11-10 2026-03-03 Sanofi CEACAM5 antibody-drug conjugate formulation
EP4046996A1 (en) 2021-02-19 2022-08-24 Universität Bielefeld Cryptophycin compounds and conjugates thereof
US11638761B2 (en) 2021-07-09 2023-05-02 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating Facioscapulohumeral muscular dystrophy
CN117980006A (zh) 2021-07-09 2024-05-03 达因疗法公司 用于治疗肌养蛋白病的肌肉靶向复合物和制剂
US11969475B2 (en) 2021-07-09 2024-04-30 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating facioscapulohumeral muscular dystrophy
US11633498B2 (en) 2021-07-09 2023-04-25 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating myotonic dystrophy
US11771776B2 (en) 2021-07-09 2023-10-03 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating dystrophinopathies
US11672872B2 (en) 2021-07-09 2023-06-13 Dyne Therapeutics, Inc. Anti-transferrin receptor antibody and uses thereof
JP2024536382A (ja) 2021-10-07 2024-10-04 サノフイ イミダゾ[4,5-c]キノリン-4-アミン化合物及びそのコンジュゲート、それらの調製並びにそれらの治療用途
KR20250004770A (ko) 2022-04-15 2025-01-08 다인 세라퓨틱스, 인크. 근긴장성 이영양증을 치료하기 위한 근육 표적화 복합체 및 제제
KR20260046445A (ko) 2023-08-04 2026-04-07 사노피 이미다조[4,5-d]피리다진 화합물 및 이의 접합체, 이의 제조 및 이의 치료적 적용

Family Cites Families (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2719170A (en) 1954-07-28 1955-09-27 Du Pont Alkyl omega-carboxyalkyl disulfides and their lower alkyl esters
US4981979A (en) 1987-09-10 1991-01-01 Neorx Corporation Immunoconjugates joined by thioether bonds having reduced toxicity and improved selectivity
FI913049A0 (fi) 1988-12-22 1991-06-20 Xoma Corp Foerhindrande kopplingsmedel och foerfaranden.
US5208020A (en) 1989-10-25 1993-05-04 Immunogen Inc. Cytotoxic agents comprising maytansinoids and their therapeutic use
CA2056039A1 (en) 1991-01-22 1992-07-23 Philip L. Fuchs Carbacyclin analogs
AU723652B2 (en) 1993-12-21 2000-08-31 University Of Hawaii New cryptophycins from synthesis
CA2264063C (en) * 1996-08-30 2007-03-13 Eli Lilly And Company Cryptophycin compounds
AU1123200A (en) 1998-10-16 2000-05-08 Eli Lilly And Company Stereoselective process for producing antineoplastic agents
WO2000034252A2 (en) 1998-12-07 2000-06-15 Eli Lilly And Company Process for the preparation of cryptophycin derivatives
JP2005511627A (ja) * 2001-11-20 2005-04-28 シアトル ジェネティクス,インコーポレーテッド 抗cd30抗体を使用する免疫学的疾患の治療
US20040249130A1 (en) * 2002-06-18 2004-12-09 Martin Stanton Aptamer-toxin molecules and methods for using same
ES2361739T3 (es) 2002-08-16 2011-06-21 Immunogen, Inc. Reticulantes con elevada reactividad y solubilidad y su uso en la preparación de conjugados para el suministro dirigido de fármacos de molécula pequeña.
US7230101B1 (en) 2002-08-28 2007-06-12 Gpc Biotech, Inc. Synthesis of methotrexate-containing heterodimeric molecules
HUE026914T2 (en) 2002-11-07 2016-08-29 Immunogen Inc Anti-CD33 antibodies and a method of treating acute myeloid leukemia
KR101145506B1 (ko) 2003-05-20 2012-05-15 이뮤노젠 아이엔씨 새로운 메이탠시노이드를 포함하는 개선된 세포독성체
KR101672664B1 (ko) 2003-07-21 2016-11-04 이뮤노젠 아이엔씨 인간화된 항체 또는 그의 항원결정기 결합절편
US20050175619A1 (en) 2004-02-05 2005-08-11 Robert Duffy Methods of producing antibody conjugates
EP1718667B1 (en) 2004-02-23 2013-01-09 Genentech, Inc. Heterocyclic self-immolative linkers and conjugates
TW200539855A (en) 2004-03-15 2005-12-16 Wyeth Corp Calicheamicin conjugates
SV2006002258A (es) 2004-10-08 2006-09-19 Wyeth Corp Inmunoterapia de trastornos autoinmunes
EP1669358A1 (en) 2004-12-07 2006-06-14 Aventis Pharma S.A. Cytotoxic agents comprising new taxanes
PL1819359T3 (pl) * 2004-12-09 2015-08-31 Janssen Biotech Inc Immunokoniugaty skierowane przeciw integrynie, metody ich wytwarzania oraz ich zastosowanie
US7385028B2 (en) 2004-12-22 2008-06-10 Ambrx, Inc Derivatization of non-natural amino acids and polypeptides
CA2600418A1 (en) 2005-03-07 2006-09-14 Archemix Corp. Stabilized aptamers to psma and their use as prostate cancer therapeutics
US7714016B2 (en) 2005-04-08 2010-05-11 Medarex, Inc. Cytotoxic compounds and conjugates with cleavable substrates
ATE527262T1 (de) 2006-01-25 2011-10-15 Sanofi Sa Neue tomaymycin derivate enhaltende zytotoxische mittel
EP1832577A1 (en) 2006-03-07 2007-09-12 Sanofi-Aventis Improved prodrugs of CC-1065 analogs
WO2007127440A2 (en) 2006-04-27 2007-11-08 Intezyne Technologies, Inc. Heterofunctional poly(ethylene glycol) containing acid-labile amino protecting groups and uses thereof
EP1864682A1 (en) 2006-06-09 2007-12-12 Sanofi-Aventis Leptomycin derivatives
EA020324B1 (ru) 2006-07-18 2014-10-30 Санофи-Авентис АНТИТЕЛА К РЕЦЕПТОРУ ЭФРИНА EphA2 И ИХ ПРИМЕНЕНИЕ
EP1914242A1 (en) 2006-10-19 2008-04-23 Sanofi-Aventis Novel anti-CD38 antibodies for the treatment of cancer
CN104383553A (zh) * 2007-06-25 2015-03-04 恩多塞特公司 含有亲水性间隔区接头的共轭物
SI2019104T1 (sl) 2007-07-19 2013-12-31 Sanofi Citotoksična sredstva, ki obsegajo nove tomaimicinske derivate, in njihova terapevtska uporaba
EP2185188B1 (en) 2007-08-22 2014-08-06 Medarex, L.L.C. Site-specific attachment of drugs or other agents to engineered antibodies with c-terminal extensions
KR101674097B1 (ko) 2008-04-11 2016-11-08 시애틀 지네틱스, 인크. 췌장, 난소 및 다른 암의 검출 및 치료
RU2487877C2 (ru) 2008-04-30 2013-07-20 Иммьюноджен, Инк. Высокоэффективные конъюгаты и гидрофильные сшивающие агенты (линкеры)
EP2281006B1 (en) 2008-04-30 2017-08-02 Immunogen, Inc. Cross-linkers and their uses
WO2010014812A2 (en) 2008-07-30 2010-02-04 The Research Foundation Of State University Of New York Peptide compositions and methods of use

Also Published As

Publication number Publication date
US20120225089A1 (en) 2012-09-06
CO6430462A2 (es) 2012-04-30
TW201110986A (en) 2011-04-01
US8952147B2 (en) 2015-02-10
TN2011000636A1 (fr) 2013-05-24
UY32745A (es) 2011-01-31
NZ597136A (en) 2014-04-30
ZA201109537B (en) 2013-03-27
HN2011003414A (es) 2014-11-10
IL217208A (en) 2016-02-29
ECSP11011553A (es) 2012-01-31
MA33465B1 (fr) 2012-07-03
CL2011003229A1 (es) 2012-06-29
CA2766762A1 (fr) 2011-01-06
NI201100219A (es) 2012-05-23
SG10201607595WA (en) 2016-11-29
FR2947271A1 (fr) 2010-12-31
CR20110670A (es) 2012-02-09
IL217208A0 (en) 2012-03-01
SG177419A1 (en) 2012-02-28
EP2448929A1 (fr) 2012-05-09
KR20120101981A (ko) 2012-09-17
MY156684A (en) 2016-03-15
CN102482238A (zh) 2012-05-30
WO2011001052A1 (fr) 2011-01-06
MX2011013764A (es) 2012-05-22
KR101770584B1 (ko) 2017-08-24
CN102482238B (zh) 2015-08-12
EA024627B1 (ru) 2016-10-31
DOP2011000376A (es) 2012-01-15
JP2012531459A (ja) 2012-12-10
AU2010267917B2 (en) 2016-03-17
JP5746692B2 (ja) 2015-07-08
CA2766762C (fr) 2017-06-20
FR2947271B1 (fr) 2013-04-05
AU2010267917A1 (en) 2012-02-02
AR078131A1 (es) 2011-10-19
BRPI1015131A2 (pt) 2018-12-04
SV2011004086A (es) 2012-05-08
FR2947269B1 (fr) 2013-01-18
EA201270096A1 (ru) 2012-07-30
FR2947269A1 (fr) 2010-12-31

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